A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522587



Internal ID15449880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:112400582..112405182hg38UCSC Ensembl
Innerchr6:112721784..112726384hg19UCSC Ensembl
Innerchr6:112828477..112833077hg18UCSC Ensembl
Innerchr6:112828477..112833077hg17UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg384601
hg194601
hg184601
hg174601
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705974
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522587
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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